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 Sure, here are some key points regarding a sink air lock in a pharmaceutical company, explained in Hinglish: Role : Sink air lock, ek aisa air lock hota hai jiski khaas design hai, jisse pharmaceutical company mein contaminants ka phailav rok sakte hai aur manufacturing environment ka integrity maintain kar sakte hai. Location: Sink air locks generally woh jagah mein lagaye jaate hai jahaan pharmaceutical products prepare kiye jaate hai, jaise ki clean rooms, laboratories aur manufacturing facilities. Design: Sink air locks mein do darwaze hote hai jo ek saath nahi khule sakte, jisse clean room se air bahar na nikal sake. Use : Clean room mein jaane se pehle, employees ko sink air lock mein apne haath aur haath ki aastein dhokar saaf karna padta hai. Saath hi unhe sahi clothing aur protective gear, jaise gloves, masks aur gowns pehnne ki zarurat hoti hai. Equipment: Sink air locks mein air showers aur HEPA filters jaise equipment bhi ho sakte hai, jo contamination risk ko aur bhi ...

Sure, here is an explanation of the cascade air lock in a pharmaceutical company, presented in Hinglish (a mix of Hindi and English) in point form: Cascade air lock ek aisa air lock system hai jo pharmaceutical manufacturing facilities mein use kiya jaata hai taaki alag-alag areas mein cross-contamination na ho. Air lock ek series of rooms ya chambers se bana hota hai jinmein interlocking doors hote hain jisse ki ek series of pressure differentials ban sake. Isse air flow ko control kiya jata hai aur contaminants ka transfer roka jaata hai. Cascade air lock ka pehla chamber gowning room hota hai, jahaan workers protective clothing pehente hain, jaise ki gowns, gloves aur masks. Dusra chamber transition room hota hai, jahaan air pressure ko lower kiya jaata hai taaki contaminants cleanroom mein na pravesh kar saken. Iss room mein pressure gowning room se kam hota hai, -10 to -15 Pascals ke beech mein hota hai. Aakhri chamber cleanroom hota hai, jahaan manufacturing ka actual kaam hota h...

Here are some basic difference between cross contamination, contamination and mix up with prevention:- Contamination: Contamination ka matlab hota hai ki kisi product ya sample mein ek anjaan cheez ya padarth ka milaavat hona. Yeh inadequate cleaning, improper storage, ya handling ki wajah se ho sakta hai. Contamination physical, chemical, ya biological nature ka ho sakta hai. Jaise ki, agar ek raaw chicken ko alag store nahi kiya jaata, toh yeh dusre foods ko bhi contaminate kar sakta hai. Contamination ko prevent karne ke liye yeh measures use kiye jaate hain: Equipment aur surfaces ko regularly clean aur sanitize karna Raw materials aur finished products ko proper storage mein rakhna Workers ko good hygiene practices follow karne ko kehna Contaminants ko regularly monitor aur test karna Cross Contamination: Cross-contamination ka matlab hota hai ki harmful bacteria ya dusre contaminants ek surface ya food se dusre surface ya food mein transfer ho jaate hain. Yeh direct contact ya in...

Granulation ka matlab hota hai granules banane ka process, jo chote, gola ya viksit aakar ke particles hote hai, jiske aamtaur par 0.2 se 4.0 mm ke beech mein size hota hai. Granulation ke process ko aksar dawai, khadya prasanskaran aur rasayan nirmaan jaise kai udyogon mein prayog kiya jaata hai. Definition:-  It is defined as the process of particle enlargement by agglomeration technique  Granulation ke kuch pramukh prakaar hote hai:- Dry granulation: Ye process ek aisa process hai jisme sukhay padartho ko thos granules mein tabdeel kiya jaata hai. Ye process tab prayog kiya jaata hai jab granulate kiya jaane wala padarth garmi ya nami ke prati sensitive ho. Wet granulation: Ye process ek aisa process hai jisme powder mishran mein ek taral binder ko milaakar granules banaye jaate hai. Ye process tab prayog kiya jaata hai jab granulate kiye jaane waale padarth ko garmi ke prati sensitive ho ya taral mein ghul kar aasani se sambhav ho. Melt granulation: Ye process ek aisa proc...

Enterprise Resource Planning (ERP) ek business management software hai, jo organizations ke day-to-day operations ko manage aur automate karne ke liye use kiya jata hai, jaise ki accounting, inventory management, production planning, human resources, aur customer relationship management. Pharmaceutical industry mein, ERP drug manufacturing aur distribution ke complex processes ko manage karne mein ek mahatvapurna role nibhata hai. Yahan par ERP ke baare mein aur jaankari ke points hai: Paribhasha: ERP ek aisa software system hai jo various business processes aur functions ko ek single, unified system mein integrate karne ke liye design kiya gaya hai. Isse business processes ko streamline karne mein madad milti hai aur isse khracha kam hota hai aur overall productivity badhti hai. Functions: Ek pharmaceutical company mein, ERP system aksar kai area ko cover karta hai jaise ki: Manufacturing: Production planning, scheduling aur manufacturing process track karna, raw material procurement ...

Pharmaceutical company mein granulation process kuch aise steps mein hota hai: Raw material preparation: Pehle sahi ingredients ko select aur prepare kiya jaata hai, jo medicine banane ke liye zaroori hai. Mixing: Ingredients ko sahi proportion mein mix kiya jaata hai, jisse mixture banta hai. Wetting: Mixture mein wetting agent add kiya jaata hai, jisse particles ek dusre se stick karte hain. Granulation: Mixture ko granulator se guzaraya jaata hai, jisse mixture ke particles chote ho jaate hain aur granules ki shape mein ban jaate hain. Drying: Granules ko sukhaya jaata hai, taaaki unme se koi extra moisture nahi rahe aur woh stable aur free-flowing ho jaaye. Milling: Granules ko desired size mein break down kiya jaata hai. Blending: Final formulation ke liye zaroori aur extra materials ko mix kiya jaata hai. Compression: Granules ko tablets ya capsules ki shape mein banaya jaata hai, jo phir coating aur packaging ke liye use kiye jaate hain. Iss process ke dauraan quality control me...

Here are the differences between qualification and validation in a simplified Hinglish language: Definition: Qualification: Iska matlab hai ki machines aur systems ko check karna hai ki woh specifications ke according set up kiye gaye hai aur sahi tarah se kaam kar rahe hai. Validation: Iska matlab hai ki processes aur products ka check karna hai ki woh consistent quality produce kar rahe hai aur standards ko meet kar rahe hai. Scope: Qualification: Yeh manufacturing mein use hone wali machines aur systems se related hai, jaise production equipment, utilities, aur facilities. Validation: Yeh manufacturing processes aur products se related hai, jaise manufacturing processes, analytical methods, aur cleaning processes. Purpose: Qualification: Iska purpose hai ki machines aur systems ko production mein use se pehle sahi tarah se set up aur functioning kiya jaye. Validation: Iska purpose hai ki processes aur products ki quality consistent ho aur standards ko development aur production ke t...

RMG aur FBD machines hai jinka use pharmaceutical companies mein powders aur granules ko mix aur dry karne ke liye kiya jata hai. RMG ka volume liters mein measure kiya jata hai kyunki yeh machine ki capacity ko indicate karta hai, jabki FBD ka weight kilograms mein measure kiya jata hai kyunki yeh material ke mass ko indicate karta hai. Consistent measurement units pharmaceutical manufacturing mein accuracy aur quality ke liye important hai. RMG ke liye liters aur FBD ke liye kilograms ka use materials ke physical properties se related hai. Powders ka density low hota hai aur zyada space occupy karte hai, isliye inka measurement liters mein kiya jata hai. Lekin granules dense hote hai aur inka measurement kilograms mein kiya jata hai. Consistent measurement units sahi records maintain karne aur traceability aur accountability ko ensure karne mein help karta hai. Iske alawa, yeh manufacturing process mein confusion aur errors ko avoid karne mein help karta hai aur measurements ka clear...

 Sure, here's a list of top pharmaceutical companies in easy Hinglish language along with their USFDA regulatory approval year: Pfizer - Ye duniya ki sabse badi dawai company mein se ek hai. Iski sthapana 1849 mein hui thi aur iska mukhyaalaya New York City mein hai. Iski kuch prasiddh dawaiyon mein Lipitor, Viagra aur Lyrica shaamil hain. Pfizer ko 1950 se pehle se hi kei USFDA approvals prapt hue hai. Johnson & Johnson - Ye ek bahumukhi American company hai jo medical devices, dawai aur consumer goods par visheshagya hai. Iska mukhyaalaya New Brunswick, New Jersey, USA mein hai. Iski kuch prasiddh dawaiyon mein Remicade, Stelara aur Imbruvica shaamil hain. Johnson & Johnson ko 1931 se pehle se kei USFDA approvals prapt hue hai. Roche - Roche ek Swiss multinational pharmaceutical company hai jiska nirmaan 1896 mein hua tha. Iska mukhyaalaya Basel, Switzerland mein hai. Iski kuch prasiddh dawaiyon mein Tamiflu, Herceptin aur Avastin shaamil hain. Roche ko 1938 se pehle se k...

Here are the principles, working principles, construction of moisture analyzer in a pharmaceutical company  Principles:- Moisture analyzer mein hum LOD principle ka use karte hai, jisse hum sample ke moisture content ko measure karte hai. Is principle mein sample ko garam kiya jata hai aur jab moisture evaporate hota hai toh sample ki weight loss ki measurement ki jati hai. Working principle:- Moisture analyzer sample ko ek specific temperature tak garam karta hai aur uske weight loss ko measure karta hai jisme moisture evaporate hota hai. Instrument ek highly accurate balance ka use karta hai, jisse sample ke weight ko before and after heating ke time par measure kiya jata hai. Moisture analyzer sample ke weight loss ke basis par moisture content ko calculate karta hai. Construction:- Moisture analyzer usually ek heating chamber, ek weighing system aur ek control system se bana hota hai. Heating chamber sample ko hold karne ke liye design kiya jata hai aur use desired temperature ...

HEPA filters bahut important hota hai pharmaceutical companies ke cleanrooms aur critical environments ke liye. Yahan kuchh easy points hai jo HEPA filters ke baare mein batate hai:- Kaam: HEPA filters kaam yeh hai ki woh air se particles aur contaminants ko remove karte hai. Yeh filters 0.3 microns tak ke particles ko bhi capture kar sakte hai aur efficiency 99.97% se upar hoti hai, jisse cleanroom ka air contaminants se free rehta hai. HEPA filter ke types: HEPA filters ke 2 types hote hai: Type A aur Type B. Type A filters non-volatile applications ke liye use kiye jaate hai, jabki Type B filters volatile applications mein use kiye jaate hai jahan explosion ka risk hota hai. Placement: HEPA filters typically air handling units (AHUs) aur terminal filter units (TFUs) mein place kiye jaate hai, jisse cleanroom ke air clean ho jaate hai. Maintenance: HEPA filters ko regular maintenance ki zaroorat hoti hai taki woh optimal level par function kar sake. Isme periodic testing, filter repl...

Here are some points explaining the concept of a Central Effluent Treatment Plant (CETP) in a pharmaceutical company, in simple Hinglish language: CETP ek aisa facility hota hai jo pharmaceutical companies mein use kiya jaata hai jahaan par paani ko treatment kiya jaata hai, taki woh environment mein jaane se pehle saaf ho jaaye. CETP typically ek central location mein hota hai company ke premises ke andar jahaan se plant ke various sources se waste water receive hota hai. Different sources se waste water ko underground pipes ke zariye CETP tak collect kiya jaata hai. CETP, screening, sedimentation, filtration aur biological treatment jaise processes use karta hai jisse waste water se contaminants aur pollutants remove ho jaate hai. Saaf kiya hua waste water, local regulatory standards ke accordance mein environment mein discharge kiya jaata hai. CETP, pharmaceutical manufacturing process ke environmental impact ko reduce karne mein help karta hai kyunki yeh waste water ko saaf karta h...

Here are some points about an Effluent Treatment Plant (ETP) in a pharmaceutical company in easy Hinglish: Purpose: ETP ka kaam hai ki wah pharmaceutical company ki manufacturing process se aati hui paani ki treatment kare, taki wah environment me jaane se pehle sahi tarah se treat ho jaaye. Treatment process: ETP physical, chemical aur biological process ka use karke paani ki treatment karta hai. Ye process paani ke composition par depend karta hai. Primary treatment: Primary treatment me paani se solid aur oil ko hataya jaata hai, jisse sedimentation aur filtration jaise physical process se kiya jata hai. Secondary treatment: Secondary treatment me dissolved organic matter aur contaminants ko activated sludge ya aerobic digestion jaise biological process se hataya jaata hai. Tertiary treatment: Tertiary treatment me chemical process jaise disinfection aur membrane filtration se baaki contaminants ko hataya jaata hai. Monitoring: ETP system ko continuously monitor kiya jaana chahiye, ...

 Sanitization of drain points in the pharmaceutical industry is important to prevent the buildup and spread of harmful bacteria and other microorganisms. Here are some common parts of drain points that may need to be sanitized in simple Hinglish language: Drain covers - Yeh cheezain drain ke muh band karne ke liye hoti hain. Inko regularly clean karna zaruri hai, taki koi bhi debris ya bacteria buildup na ho. Drain pipes - Yeh pipes drain tak jaate hain, inhe sanitize karna bhi zaruri hai taki bacteria aur harmful microorganisms nahi ban payein. P-traps - Yeh pipes curve ke shape mein hote hain, aur inka kaam hota hai odors ko rokna drain se upar aane se. Inme debris build up ho jata hai, toh inhe clean karna ya replace karna zaruri hai. Floor drains - Yeh drains floor par hotey hain. Inhe regularly clean karna zaruri hai, taki bacteria aur debris build up na ho. Sanitary fittings - Yeh fittings drain pipes ko connect karne ke liye hotey hain. Inhe clean aur sanitize karna zaruri h...

Disinfectants aur sanitizing agents dono hi pharmaceutical companies mein use kiye jaate hain, jisse ek saf aur steril environment maintain kiya ja sake. Inn dono ke beech kuch differences hote hain: Ingredients: Disinfectants mein bleach, hydrogen peroxide, ya quaternary ammonium compounds jaise chemicals hote hain, jo ki microorganisms ko kill ya inactivate karne ke liye design kiye jaate hain. Jaise, agar kisi lab ki bench ya production equipment mein zyada saare bacteria hote hain, toh disinfectant unko destroy karne mein helpful hota hai. Sanitizing agents mein alcohol, chlorine dioxide, ya peracetic acid jaise mild chemicals hote hain, jo ki microorganisms ke numbers ko safe levels tak reduce karne ke liye design kiye jaate hain. Jaise, agar kisi production line par food ya dusre products ke contact ke kaaran bacteria hote hain, toh sanitizing agent unhein kam karne mein helpful hota hai. Mechanism of action: Disinfectants kaam karne ke liye microorganisms ke cell walls, membrane...

Deviation ka matlab hota hai ki koi likhit procedure ya standard operating procedure (SOP) ke khilaaf chalna ek pharmaceutical company mein. Ye kisi bhi manufacturing process ke kisi bhi stage mein ho sakta hai, jaise ki raw material procurement se lekar finished product ki release tak. Deviation ke prakaar: Minor Deviation - Agar koi minor deviation likhit procedure se hota hai jo product ki quality ya safety ko influence nahi karta hai, toh use minor deviation kehte hai. Major Deviation - Agar koi significant deviation likhit procedure se hota hai jo product ki quality ya safety ko influence kar sakta hai, toh use major deviation kehte hai. Critical Deviation - Agar koi bahut hi serious deviation likhit procedure se hota hai jo product ki quality ya safety ko bahut bada nuksaan pahucha sakta hai, toh use critical deviation kehte hai. Deviation ka uddeshya: Deviation ka uddeshya hai ki uska root cause pata lagakar use correct karna. Deviation ke impact ko product ki quality aur safety...

Verification aur calibration dono pharmaceutical industry me important processes hai. Inka use alag alag hai aur inme kuch differences hai:- Verification ka matlab hai ki kisi equipment ya process ko uske standards ya requirements ke according verify karna. Calibration ka matlab hai ki kisi equipment ya instrument ke output ko ek known standard se compare karna, jisse uski accuracy determine ki ja sake. Verification ka purpose hai ki ek instrument ya equipment uske intended use ke according function kar raha hai aur reliable results produce kar raha hai. Calibration ka purpose hai ki ek instrument ya equipment ki accuracy aur precision determine ki jaye aur agar zarurat ho to use adjust kiya jaye. Verification ki frequency regular hoti hai, jaise ki daily, weekly ya monthly, taki equipment hamesha accurate results produce kare. Calibration less frequent hoti hai, jaise ki annually ya biannually, instrument ya equipment ke hisab se. Verification me ek simple check ya test se instrument ...

In the context of pharmaceutical companies, the terms "dynamic record," "static record," and "manual record" typically refer to different types of documentation related to various aspects of the drug development and manufacturing process. Here's a breakdown of each term and what it typically entails: Dynamic record: Ek dynamic record kisi bhi prakar ka electronic record hai jo dawa vikas ke dauran banaya, badla ya hataya jata hai. Ye records aam taur par database ya doosre electronic system mein store kiye jate hain aur laboratory test results, production batch records, aur quality control data jaisi jaankari shamil ho sakti hai. Dynamic records aam taur par real-time mein update kiye jaate hain aur dawa vikas ke prakriya ko monitor karne, sambhavit mudde ko pahchanne aur sabse up-to-date jaankari ke aadhaar par faisla lene ke liye istemaal kiye jaate hain. Static record: Ek static record kisi bhi prakar ka electronic record hai jo kisi vishesh samay k...

Here are the various types of documents in pharmaceutical company:- Standard Operating Procedures (SOPs): SOPs ek tarah ki likhit pranali hai jo batati hai ki kisi vishesh task ya operation ko kaise standard tarike se perform karna hai. Ye pharmaceutical products ki production mein consistency aur quality ko ensure karne ke liye use hoti hai. SOPs ek pharmaceutical company mein bahut zaroori hai kyunki regulatory requirements ke saath compliance ko maintain karne mein help karti hai aur saath hi products ki safety aur efficacy ko bhi ensure karti hai. Conclusion ye hai ki SOPs critical documents hai jo ek pharmaceutical company mein develop aur implement kiye jaana chahiye. Batch Records: Batch records ek tarah ke documents hai jo kisi specific batch ke drug product ki manufacture ki puri history provide karta hai. Ismein raw materials used, manufacturing process, testing procedures, aur quality control tests ke results ke baare mein information hoti hai. Batch records ko use kiya jaat...

Here are the details you asked for about the first pharmaceutical company in India: Established Year: The first pharmaceutical company in India was established in the year 1901. Owner : The company was founded by Khwaja Abdul Hamied, a visionary entrepreneur who wanted to bring affordable medicines to the Indian people. Name : The name of the company is "Cipla" which stands for "Chemical, Industrial & Pharmaceutical Laboratories". Turnover : Cipla has grown to become one of the largest pharmaceutical companies in India, with a turnover of over $2 billion USD in 2021. Products : Cipla manufactures a wide range of pharmaceutical products including prescription drugs, over-the-counter medications, and veterinary products. Some of its most well-known products include respiratory inhalers, antiretroviral drugs for HIV/AIDS, and cancer treatments. Headquarters : Cipla is headquartered in Mumbai, India, and has operations in over 80 countries around the world. Overall,...

Here are the differences between purified water and potable water in the context of the pharmaceutical industry in Hinglish: Purified Water: Purified water woh pani hai jo ek khareedaari ki safai prakriya se guzarti hai jisme kitanu, ghul jaane wale padarthon aur prakritik tatvon jaise saare anishchit tatva ko hata diya jata hai. Udharan: Purified water utpaadon ki gunvatta ko prabhaavit karne waale anuchit tatvon se mukt hone ke liye ulta osmosis, deionization aur distillation jaise prakriyaaon ke maadhyam se taiyar kiya ja sakta hai. Purified water ke paas ek dhimaakhaadh pH maatra 7 hoti hai aur yeh ion, dhaatu aur anya padarthon se mukt hoti hai jo dawaaiyon aur chikitsa upakaranon se sampark karne mein sankramit hone ki sambhavna rakhte hain Udharan: Purified water ka pH level utpaadon ki sthirata aur ekta ke liye dhyaan se niyantrit kiya jata hai. Purified water dawaaiyon ko gholne aur dubaane, upakaranon ki saaf-safai karne aur containers ko dhone jaise aadhaar-shila upakaranon ...

All about SS316 their identification test, ingredients, applications and all:-  SS316 ki identification test procedure: Visual inspection se material ke surface condition, dimensions, aur markings verify ki jati hai. Chemical analysis se material ke composition ka pata lagaya jata hai, jisme chromium, nickel, molybdenum, aur carbon ka percentage shaamil hota hai. Mechanical testing se material ki strength, hardness, aur ductility ka moolyaankan kiya jata hai. Non-destructive testing se material ke defects, cracks, ya koi dusri kamiyan pata lagayi jati hai. SS316 ke ingredients: SS316 ek prakar ka stainless steel hai jisme ye ingredients shaamil hote hain: 16-18% Chromium 10-14% Nickel 2-3% Molybdenum 0.08% Carbon SS316 ke applications: SS316 aam taur par pharmaceutical industry mein kuch aise applications ke liye istemaal kiya jata hai: Bioprocessing equipment jaise tanks, reactors, aur piping systems Surgical instruments aur implants Pharmaceutical packaging aur storage containers...

Here are the differences between OOT and OOS with a focus on their importance, principles, application, role, and responsibility: 1.Importance: OOT aur OOS davaon ki quality aur safety ka dhyan rakhne ke liye mahatvapurn hai. Inse pata chalta hai ki dawa ki utpadan prakriya, raw materials ya phir purn utpadan mein koi samasya hai jisse dawa ki karya-kshamta aur suraksha prabhavit ho sakti hai. 2.Principles: OOT prakriya mein data ko samay ke saath track kiya jaata hai taaki joote hue range ke bahar jaane wale kisi bhi badlav ko pehchaan saken. Jabki OOS prakriya mein davaon ke liye nirdharit quality standards aur specifications ko pura kiya jaata hai. 3.Application: OOT aam taur par davaon ke vikas aur parikshan avdhiyon mein prayog kiya jaata hai, jabki OOS utpadan aur parikshan avdhiyon mein prayog kiya jaata hai jisse ye sahi quality standards ko poora karte hai. 4.Role: OOT samasyaon ko pehchaanne mein madad karta hai jaldi hi, jisse wo bade masle mein badalne se pehle hi nipat jaa...

Here are 10 basic points difference between BMR and BPR:-  BMR (Batch Manufacturing Record) aur BPR (Batch Packaging Record) do mahatvapurn dastavij hain jinhe pharmaceutical manufacturing process me upyog kiya jata hai. BMR ka uddeshya ek dawai ke utpadan prakriya ko darj karna hai, jabki BPR ka uddeshya usi utpad ki packaging prakriya ko darj karna hai. BMR utpadan prakriya ke vivaran jaise upayog kiye gaye kacche maal, prakriya ke kadam aur gunavatta niyantran ki jaankari shaamil karta hai, jabki BPR packaging prakriya ke vivaran jaise packaging saaman, labelling aur storage sthiti shaamil karta hai. BMR banane ke liye utpadan vibhaag zimmedar hota hai, jabki BPR banane ke liye packaging vibhaag zimmedar hota hai. BMR ko utpadan prakriya shuru hone se pahle quality control vibhaag dvara maanyata prapt honi chahiye, jabki BPR ko packaging prakriya shuru hone se pahle quality control vibhaag dvara maanyata prapt honi chahiye. Kisi bhi parivartan ko BMR me darj kiya jaana chahiye a...

Sure, here is an explanation of 483a observation by the USFDA in a pharmaceutical company, presented in easy Hinglish bullet points: USFDA ki ek team pharmaceutical companies ko inspect karti hai, agar unko koi kami ya galat kaam nazar aata hai, toh woh 483a observation naam ki ek report banati hai. Is report mein FDA ki team ne company ke kaam mein ki gayi kamiyan ya galatiyon ko likha hota hai, jismein se kuch kamiyan behad serious hoti hai. Is report mein company ke kaam ke kuch aise tukde bhi hote hai, jinmein koi kami nahi hai, par overall dekha jaye toh unki performance kamzor hoti hai. Is report mein company ko bataya jata hai ki kis area mein unka kaam FDA ke rules aur regulations ke khilaaf hai. Is report mein company ko woh bhi bataya jata hai ki woh kya karein jisse woh galati ko theek kar sakein. Company ko ek time limit diya jata hai, jismein woh apni galti ko sudhaar ke FDA ko report karna hota hai. Agar company apni kamiyon ko theek nahi karti hai, toh FDA aur bhi sakht ...

Sanitalk  Here are top 8 unknown facts about pharmaceutical manufacturing company:- 1.Bharat mein generic dawaiyon ka utpadan bahut bada hai. Yahaan par kai pramukh dawai banane ki company hain jaise ki Sun Pharmaceutical Industries, Dr. Reddy's Laboratories aur Cipla. 2. Sarkar dvaara bahut adhik niyamit kiya jaata hai aur is industry par kadi niyantran kiya jaata hai. Bharat ke dawa industry ka karobar lagbhag 41 arab dollar ka hai aur iski aane waale 11-13% ke growth ka anumaan hai. 3.Bharat ki dawa industry duniya bhar mein 200 deshon mein dawaon ki niryat karti hai aur viksit deshon jaise ki America aur Europe mein generic dawaon ki badi chaadar hai. 4.Bharat ke dawa banane ki company adhyayan aur vikas par bahut dhyaan dete hain. Kai companies ke paas unke khud ke adhyayan aur shodh sansthaan hain, jinhone academic institutions aur research organizations ke saath sahayog bhi kiya hai. 5.Bharat ke kai dawa banane ki company badi sankhya mein aisi dawaiyan banaati hain jo badi ...

Sure, here is the principle, definition, parts, and applications of sling hygrometer in easy Hinglish language: Principle : Sling hygrometer air ki relative humidity ko measure karne ke liye use hota hai. Ye kaam do thermometer ki readings compare karke karta hai, ek sukhra aur ek bhiga hua. Bhige hue thermometer ko ek bhigoyi hui wick ya fabric se cover kiya jata hai, jisme se pani evaporate hote hue cooling hoti hai, jabki sukhra thermometer sukh rahta hai. Definition : Sling hygrometer ek aisa device hai, jise air ki relative humidity ko measure karne ke liye use kiya jata hai. Isme do thermometer handle par mount kiye jate hai, jisme se ek sukhra hota hai aur dusra bhiga hua. In dono thermometer ke readings ko compare karke relative humidity calculate ki jati hai. Parts : Do thermometer (wet aur dry bulb ) Wet hue thermometer ko cover karne ke liye wick ya fabric Handle device ko hold karne ke liye Temperature readings ko relative humidity mein convert karne ke liye chart ya table ...

Hygrometers humidity ko measure karne ke liye use kiye jaane wale devices hai. Neeche diye gaye hain hygrometers ke principle, types aur pharmaceutical companies mein inke applications: Hygrometers ke Principle: Absorption Principle: Is principle ke anusar kuch cheezein jaise baal, paper aur namak aasman se nami ko absorb karte hain, jisse inki size ya shape badal jaati hai. Inke size ya shape ke badalne se humidity ki measurement hoti hai. Electrical Principle: Is principle mein substance ki electrical conductivity ya dielectric constant ko use kiya jata hai, jisse humidity ki measurement ki jaati hai. Hygrometers ke Types:  Mechanical Hygrometers: Ye absorption principle par based hai aur hygroscopic substance jaise baal, paper ya namak ka use hota hai, jisse humidity ki measurement hoti hai. Electrical Hygrometers: Ye electrical principle par based hai aur resistive, capacitive aur thermal conductivity hygrometers ismein aate hain. Optical Hygrometers: Ye moisture ko absorb karn...

Here are the types of air used in pharmaceutical companies, their applications, and their limits explained in easy-to-understand Hinglish: Compressed air: Kuch machines, jaise packaging machines, filling machines aur conveyors chalane ke liye compressed air ka istemal hota hai. Is air me oil aur gandagi nahi honi chahiye taaki product ko contamination se bachaya ja sake. Pressure ko equipment aur product quality ke liye safe rakha jana chahiye. Filtered air: Filtered air manufacturing aur packaging areas ke liye clean air provide karne ke liye istemal hota hai. Is air me moujood gandagi aur impurities ko filter karne ke liye use kiya jata hai. Filters ko regular basis par saaf kiya jana chahiye taaki air clean bani rahe. Sterile air: Sterile air filling areas aur kuch critical areas ko sterile banaye rakhne ke liye istemal hota hai. Is air me microorganisms na ho, taaki product contamination se bachaya ja sake. Sterile air produce karne ke liye istemal kiya jane wala equipment tested h...

  Aaj kal duniya mein bahut saare pharmaceutical manufacturing companies hain. Inme se kuch companies accessories coding ka use karti hain. Yeh process equipment aur materials ko unique codes dene ka process hai. Ismein kuch important points hain: Identification : Accessories coding se equipment aur materials ko identify karna asaan ho jaata hai. Traceability :Coding system ka use karke, manufacturing process ke har stage ki history trace karne mein asaani hoti hai. Yeh regulatory requirements ke saath product quality aur safety ke liye important hai. Inventory management: Accessories coding inventory level aur materials aur equipment usage ko track karne mein helpful hoti hai. Maintenance : Equipment aur accessories ko unique codes dene se maintenance schedule track karne aur equipment ko sahi se maintain karna asaan ho jaata hai. Pharmaceutical manufacturing mein do tarah ke coding systems hote hain: Barcode : Barcoding bahut common coding system hai jismein labels ya tags par un...

Here are the cleanroom classifications according to different regulatory bodies:- 1.ISO Cleanroom Classification:- ISO organization ke dwara banai gayi ye classification ka use particle count ko define karne ke liye kiya jata hai. Is classification ke anusar cleanroom ka level particles per cubic meter of air ke upar nirbhar karta hai. Isme kuch alag alag classes hai jisme particles ke size ke anusar maximum allowable particle count fix kiya jata hai. The classifications are as follows: ISO Class 1: Maximum 10 particles per cubic meter (≥0.1 μm) ISO Class 2: Maximum 100 particles per cubic meter (≥0.1 μm) ISO Class 3: Maximum 1,000 particles per cubic meter (≥0.1 μm) ISO Class 4: Maximum 10,000 particles per cubic meter (≥0.1 μm) ISO Class 5: Maximum 100,000 particles per cubic meter (≥0.1 μm) ISO Class 6: Maximum 1,000,000 particles per cubic meter (≥0.1 μm) ISO Class 7: Maximum 352,000 particles per cubic meter (≥0.5 μm) ISO Class 8: Maximum 3,520,000 particles per cubic meter (≥0.5 ...

Good housekeeping practices ko ek pharmaceutical company mein follow karna bohot zaruri hai, taki kaam karne ka environment safe aur efficient rahe. Yahaan kuch key points hai jinhe consider karna chahiye: 1.Cleanliness : Kaam karne ka environment saaf rakhna kaafi zaruri hai taaki dust, dirt aur other contaminants ka buildup na ho jisse product ki quality affect ho sake. 2.Organization : Equipment, tools aur materials ko proper organize karna accidents ka risk kam karta hai aur jab zarurat ho tab items locate karna bhi easy ho jaata hai. 3. Waste Management : Waste materials jaise chemicals, packaging aur other materials ko properly manage karna chahiye taaki hazardous waste ka buildup na ho workplace mein. 4. Personal Protective Equipment (PPE): Employees ko necessary PPE jaise gloves, safety goggles aur face masks provide karna chahiye taki unhe hazardous chemicals aur biological agents se protect kiya ja sake. 5.Storage : Raw materials, finished products aur other materials ko des...

Material Safety Data Sheets (MSDS) ke bahut maayne hote hain pharmaceutical manufacturing industry mein jahan par chemicals aur dusre khatarnak materials ka istemaal kiya jaata hai. Yahan kuch important points MSDS ke baare mein hinglish language mein bataye gaye hain: 1.Safety of woorkers :- MSDS mein chemicals aur dusre khatarnak materials ke saath judi sambhav khatron ke baare mein jaankari hoti hai jo ki karmachaariyon ko sahi suraksha ke liye sahi precautions lene mein madad karti hai. 2.Compliance : MSDS, Occupational Safety and Health Administration (OSHA) regulations ke tahat ek legal requirement hai United States mein aur dusre deshon mein bhi similar regulations hote hain. Noncompliance fine aur dusre penalties se sambandhit hota hai. 3.Emergency Preparedness: MSDS, khatarnak materials ke spill, fire, ya dusre emergency situations mein sahi response procedures ke baare mein guidance provide karta hai jisse karmachaariyon aur environment ko protect kiya jaa sakta hai. 4.Produ...

To prepare 70% Isopropyl Alcohol (IPA) V/V in a pharmaceutical company, follow these steps: Decide kitna 70% IPA V/V chahiye hai. Is formula ka istemal karke calculate karein ki kitna IPA aur pani chahiye hoga: Amount of IPA (in ml) = Required volume of 70% IPA V/V (in ml) x 0.7 Amount of water (in ml) = Required volume of 70% IPA V/V (in ml) x 0.3 Measuring cylinder ya flask ka istemal karke IPA aur pani ka measurement karein. Ek saaf container mein IPA daalein, aur dheere-dheere pani daalte rahein aur halka sa hilate rahein. Hydrometer ya refractometer ka istemal karke check karein ki solution 68% se 72% concentration ke beech hai. Container par date aur concentration ke saath label laga dein aur use se pehle clean aur dry jagah mein store karein. IPA ki purity kam se kam 99% honi chahiye aur pani mein koi bhi impurities nahi hone chahiye. Contamination se bachne ke liye saaf jagah par kaam karein aur solution ko expiry date se pehle use karein. Thank you for visiting, see you again ...

1.Definition :-  Instruments woh devices hai jo physical quantities ya variables ko measure, indicate ya control karne ke liye use kiye jaate hai jaise temperature, pressure ya flow rate. Equipment, dusri taraf, ek broader range ke devices hai jo manufacturing ya processing ke liye use kiye jaate hai. 2.Functions :- Instruments ka primary kaam physical variables ko measure aur control karna hai. Equipment specific tasks ya functions perform karne ke liye design kiya gaya hai jaise processing ya manufacturing. 3.Complexity : Instruments equipment se jyada complex hote hai, kyunki unhe apni measurements mein accuracy aur precision ke higher degree ki zarurat hoti hai.  Equipment complexity mein vary kar sakta hai, lekin generally instruments se kam complex hote hai. 4.Precision : Instruments ko precise aur accurate measurements provide karne ke liye design kiya gaya hai, often with very high levels of accuracy.  Equipment bhi precision require kar sakta hai, lekin instrumen...

PPE (Personal Protective Equipment) pharmaceutical companies mein use kiye jaate hain taaki employees ko khatra se bachaya ja sake jo ki hazardous materials ko handle, manufacture aur dispose karte time ho sakta hai. Kuch important points hain PPEs ke baare mein: 1.Definition : PPEs ka matlab hota hai protective equipment jo ki workplace hazards se associated risks ko kam karne ke liye design kiya gaya hai. Is equipment mein gloves, goggles, face shields, respirators, coveralls aur aur bhi kuch protective clothing shaamil hain. 2.Types of PPEs used in pharmaceutical companies: - Respirators: harmful substances inhale hone se employees ko bachane ke liye use kiye jaate hain. - Gloves: chemical exposure se hands ko bachane ke liye use kiye jaate hain. - Goggles aur face shields: chemical splashes aur sprays se eyes aur face ko bachane ke liye use kiye jaate hain. - Coveralls aur other protective clothing: chemical exposure se body ko bachane ke liye use kiye jaate hain. 3.Importance of u...

Pharmaceutical manufacturing companies use electronic balances to measure and weigh small amounts of materials accurately. Isme alag alag prakar ke electronic balances hote hai:- 1.Analytical Balances : Ye balances bahut hi chhote maatra ke materials ko bohot hi sahi tarike se weigh karne ke liye use kiye jaate hain, jaise active pharmaceutical ingredients. 2.Top Loading Balances : Ye balances bade maatra ke materials ko weigh kar sakte hain, jisme kuch sau gram tak ki matra shaamil ho sakti hai. 3.Micro Balances: Ye balances bahut hi chhote maatra ke materials ko weigh karne ke liye use kiye jaate hain, jisme micrograms ke range tak matra shaamil hoti hai. 4.Moisture Balances: Ye balances sample mein present moisture ki matra ko measure karne ke liye use kiye jaate hain. 5.Density Balances: Ye balances liquid aur solid materials ke density ko measure karne ke liye use kiye jaate hain. Pharmaceutical manufacturing company mein electronic balance kaunsa use kiya jaata hai, ye material...

  Sanitalk  Sure, here are five key points of the 5S methodology as applied to pharmaceutical companies, explained in simple Hinglish language: 1.Sorting (Seiri) - Is stage mein workplace mein maujood sabhi samagri ko check karna aur jo kaam nahi aata hai ya purani ho chuki hai, use nikal dena. Ek pharmaceutical company mein, is stage mein khatam hone wali medicines, purane equipments ya extra supplies ko nikal dena ho sakta hai. 2.Setting in order (Seiton) - Sort karne ke baad, agla kadam hai jo bacha hai use set karna. Ismein medicines aur lab supplies ko alag-alag rakhne ke liye jagah banani hai, shelves aur drawers ko label karna hai aur saman ko aasani se dhoondhne ke liye sahi jagah par rakhna hai. 3.Shine(Seiso) - Is stage mein workplace ko saaf-suthra rakhna hai. Ek pharmaceutical company mein, iska matlab hai ki lab equipment aur work surfaces ko regular clean karke contamination ko rokna aur accurate results ke liye saaf rakhna hai. 4.Standardize (Seiketsu) - Jab wo...

Environmental monitoring ka matlab hai ki pharmaceutical industry mein nirdhaarit avadhiyon ke anusaar, manufacturing facility mein maujood hawa, paani aur surfaces ko niyantrit roop se check karna. Iska kuchh fayde aur nuksaan niche diye gaye hain: Merits :-  Quality control: Environmental monitoring ka upayog karke, manufacturing facility mein saaf safai ka dhyaan rakhne se achchha quality ka utpaad taiyar kiya jaa sakta hai. Compliance: Environmental monitoring ka palan karna, pharmaceutical manufacturing facilities ke liye vidhiyaon ke anusaar avashyak hai, jisse companies ko jurmana aur anya dand se bacha ja sakta hai. Samasyaon ka pehle se pata chalna: Regular environmental monitoring se, samasyaon ka pehle hi pata chal jaata hai, jisse jaldi corrective action liya jaa sakta hai aur downtime kam hota hai. Safety: Environmental monitoring ke dwara, facility mein maujood kisi bhi khatra ko pahle se hi pata chal jaata hai, jisse karmachariyon aur grahakon ki suraksha bani rehti ...